Allele Registry

Canonical Allele Identifier: PA2579935331

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.151623621

Score 0.769777958

Score 1.2014966079

Score 1.1335386317

Score 0.05956961

Score -1.6504480799

Linked Data - NCBI & NCI

ClinVar Allele:

363550

ClinVar RCV:

RCV000422282

RCV000423344

RCV000424582

RCV000427043

RCV000433417

RCV000433620

RCV000434681

RCV000439990

RCV000440155

RCV000442891

RCV000442920

RCV001202958

ClinVar Variation:

376671

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Val216Gly	CA16603085 NM_000546.6:c.647T>G